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Organic Letters
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October 12, 2002
Synthesis of the C(2)-C(13) fragment (the A-B spiroketal unit) of spongistatin 1 (altohyrtin A): use of a common intermediate for the synthesis of both spongistatin spiroketals
Edward B Holson, William R Roush
Organic Letters
|
October 12, 2002
Diastereoselective synthesis of the C(17)-C(28) fragment (the C-D spiroketal unit) of spongistatin 1 (altohyrtin A) via a kinetically controlled iodo-spiroketalization reaction
Edward B Holson, William R Roush
Nature Biotechnology
|
March 11, 2011
Chemoproteomics quantifies complexity
Edward B Holson, Stuart L Schreiber
Organic Letters
|
May 9, 2003
Common-intermediate strategy for synthesis of conduritols and inositols via beta-hydroxy cyclohexenylsilanes
Jung-Nyoung Heo, Edward B Holson, William R Roush
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
October 9, 2013
Small molecule inhibitors of zinc-dependent histone deacetylases
Florence F Wagner, Michel Weїwer, Michael C Lewis, et al.
Future Medicinal Chemistry
|
September 13, 2013
Therapeutic potential of isoform selective HDAC inhibitors for the treatment of schizophrenia
Michel Weïwer, Michael C Lewis, Florence F Wagner, et al.
ACS Chemical Biology
|
January 27, 2010
Characterization of plant-derived saponin natural products against Candida albicans
Jeffrey J Coleman, Ikechukwu Okoli, George P Tegos, et al.
The Journal of Biological Chemistry
|
September 2, 2017
Isoform-selective inhibitor of histone deacetylase 3 (HDAC3) limits pancreatic islet infiltration and protects female nonobese diabetic mice from diabetes
Ercument Dirice, Raymond W S Ng, Rachael Martinez, et al.
Chemistry & Biology
|
April 21, 2015
Hydroxamate-based histone deacetylase inhibitors can protect neurons from oxidative stress via a histone deacetylase-independent catalase-like mechanism
David E Olson, Sama F Sleiman, Megan W Bourassa, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 31, 2013
Signal-dependent repression of DUSP5 by class I HDACs controls nuclear ERK activity and cardiomyocyte hypertrophy
Bradley S Ferguson, Brooke C Harrison, Mark Y Jeong, et al.
Page
of 4
Search research articles
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Showing results (1-10 of 38) with videos related to
Sort By:
Page
of 4
Organic Letters
|
October 12, 2002
Synthesis of the C(2)-C(13) fragment (the A-B spiroketal unit) of spongistatin 1 (altohyrtin A): use of a common intermediate for the synthesis of both spongistatin spiroketals
Edward B Holson, William R Roush
Organic Letters
|
October 12, 2002
Diastereoselective synthesis of the C(17)-C(28) fragment (the C-D spiroketal unit) of spongistatin 1 (altohyrtin A) via a kinetically controlled iodo-spiroketalization reaction
Edward B Holson, William R Roush
Nature Biotechnology
|
March 11, 2011
Chemoproteomics quantifies complexity
Edward B Holson, Stuart L Schreiber
Organic Letters
|
May 9, 2003
Common-intermediate strategy for synthesis of conduritols and inositols via beta-hydroxy cyclohexenylsilanes
Jung-Nyoung Heo, Edward B Holson, William R Roush
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
October 9, 2013
Small molecule inhibitors of zinc-dependent histone deacetylases
Florence F Wagner, Michel Weїwer, Michael C Lewis, et al.
Future Medicinal Chemistry
|
September 13, 2013
Therapeutic potential of isoform selective HDAC inhibitors for the treatment of schizophrenia
Michel Weïwer, Michael C Lewis, Florence F Wagner, et al.
ACS Chemical Biology
|
January 27, 2010
Characterization of plant-derived saponin natural products against Candida albicans
Jeffrey J Coleman, Ikechukwu Okoli, George P Tegos, et al.
The Journal of Biological Chemistry
|
September 2, 2017
Isoform-selective inhibitor of histone deacetylase 3 (HDAC3) limits pancreatic islet infiltration and protects female nonobese diabetic mice from diabetes
Ercument Dirice, Raymond W S Ng, Rachael Martinez, et al.
Chemistry & Biology
|
April 21, 2015
Hydroxamate-based histone deacetylase inhibitors can protect neurons from oxidative stress via a histone deacetylase-independent catalase-like mechanism
David E Olson, Sama F Sleiman, Megan W Bourassa, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 31, 2013
Signal-dependent repression of DUSP5 by class I HDACs controls nuclear ERK activity and cardiomyocyte hypertrophy
Bradley S Ferguson, Brooke C Harrison, Mark Y Jeong, et al.
Page
of 4